In the presence of equimolar quantity of BCl3, phenols 1 react with isocyanates and acyl chlorides to give, usually with good-excellent yields, 2-hydroxy-aryl-carboxy-amides 2 and 2-hydroxy-aryl-ketones 3 respectively. A distinctive behaviour of BCl3 in comparison with other Lewis acids is observed

Boron trichloride-catalyzed ortho carbonylation of phenols: synthesis of 2-hydroxyarenecarboxamides and ketones

CITTERIO, ATTILIO
1986-01-01

Abstract

In the presence of equimolar quantity of BCl3, phenols 1 react with isocyanates and acyl chlorides to give, usually with good-excellent yields, 2-hydroxy-aryl-carboxy-amides 2 and 2-hydroxy-aryl-ketones 3 respectively. A distinctive behaviour of BCl3 in comparison with other Lewis acids is observed
1986
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11311/662953
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